Journal of The Electrochemical Society · 2020 · 49 citations · 48 references
Natural SciencesChemical EngineeringMaterials ScienceElectrochemical EngineeringElectrochemistryEnergy MaterialsAnode MaterialsBattery MaterialsCathode MaterialsElectrochemical CellsElectrochemical Energy StorageElectrode MaterialsCoin Cell BatteriesDischarge CapacityHard CarbonHard Carbon AnodesLayered CathodesLayered Oxide CathodesSodium-ion BatteriesSodium-ion Cathodes
In this work, we report the practical realization of 3.6 V Sodium-ion coin and multi-electrode pouch-type cells using O3-type layered NaNi 0.5 Mn 0.3 Co 0.2 O 2 cathodes and dextrose derived hard carbon anodes in one-unit cell. The manuscript provides a thorough study of NaNi 0.5 Mn 0.3 Co 0.2 O 2 cathodes along with hard carbon anodes and its practical difficulty in the development of Sodium-ion cells. NaNi 0.5 Mn 0.3 Co 0.2 O 2 cathodes deliver an initial discharge capacity of ∼136 mAhg −1 with a moderate capacity retention of 87 mAhg −1 at 0.1C rate after 200 cycles. Similarly, the hard carbon anodes show a reversible capacity of about 280 mAhg −1 at C/10 rate. The diffusion coefficient of Sodium-ion calculated is in the order of 10 −11 –10 −12 cm 2 s −1 suggesting good reversibility, capacity retention and C-rate performance of the cathode. Further, no change in peak voltage in dQ/dV plots, XRD patterns, and CVs dictates the crystalline phase stability of NaNi 0.5 Mn 0.3 Co 0.2 O 2 during cycling. NaNi 0.5 Mn 0.3 Co 0.2 O 2 retains good structural stability during long cycling and decreased interlayer transition metal ion migration. Engineering aspects for assembling and testing O3-Type NaNi 0.5 Mn 0.3 Co 0.2 O 2 -hard carbon in the full cell is also investigated thoroughly. Herein, we have taken the research output and challenges from the coin-type cell and applied further to develop single and multi-electrode pouch type-cell of various configurations.
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